Regulatory Affairs Associate
2 months ago
**Details**:
- Full-time permanent position
- Hybrid working - 3 days WFH, 2 days office (Surrey)
- Competitive package
- Global pharma company
**The Role**:
**Objective / Purpose of Role**
To support the Regulatory Affairs function of the Operations department, carrying out a range of tasks supporting the fulfillment of responsibilities of the Marketing Authorisation Holder for the product portfolio, working with Quality Assurance, Medical Affairs, and external contractors.
**Key Activities / Key Responsibilities**
- Regulatory filing and administration
- Communication of regulatory changes internally and externally
- Generation, review and implementation of Product Information (Summary of Product Characteristics, leaflets and labelling)
- Review and processing of certificates of analysis for received product batches
- Review of stability reports, annual Product Quality Reviews, SOPs, other technical documents and change controls
- Review and support updates to product Artwork
- Handling Product Quality Complaints
- Degree in Pharmacy, Chemistry, Pharmaceutical or life sciences
- Life Science industry, e.g. regulatory affairs function.
- Minimum 1 year UK regulatory experience - ideally experience in variations, labelling and artwork changes
- Salary/Rate: Competitive salary, bonus and benefits
- Contract Type: Permanent - Full Time
- Start Date: ASAP - permanent role
- Location: Hybrid working - 2 days office (Surrey), 3 days WFH
- Reference: 0911RAAM**Apply**:
If you feel that you are qualified for this position please apply.
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